Allele Registry

Canonical Allele Identifier: PA281899

Gene: TGFB2 HGNC NCBI

ClinVar RCV:

RCV000030732

ClinVar Variation:

37085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129071.1:p.Pro366His	CA281898 NM_001135599.4:c.1097C>A